DisGeNET - a database of gene-disease associations

List of associated variants

Waist-Hip Ratio, C0205682

Source: ALL

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs2061708	COL11A1	1	102951647	intron variant	G/A;C;T	snv			2
rs2298632	TCEA3	1	23383982	3 prime UTR variant	C/T	snv		0.40	2
rs3851294	DSTYK	1	205161285	missense variant	A/G;T	snv	0.93		2
rs4846565	LYPLAL1-AS1	1	219548762	intergenic variant	G/A	snv		0.26	2
rs505102	CFH	1	196650372	upstream gene variant	T/C	snv		0.40	2
rs10458575		1	65104082	regulatory region variant	T/C	snv		0.45	1
rs10752944	DNM3 ; LOC102724528 ; PIGC	1	172394384	non coding transcript exon variant	C/T	snv		0.47	1
rs10863961	PPP2R5A	1	212294505	intron variant	G/A	snv		0.24	1
rs10875120	LINC01930 ; DPYD ; MIR137HG	1	97934347	intron variant	G/T	snv		0.72	1
rs10927263	NID1	1	236017804	intron variant	A/G	snv		0.30	1
rs11204762	PRUNE1	1	151027261	synonymous variant	A/G	snv	0.25	0.24	1
rs116565273	WARS2-AS1	1	119260389	non coding transcript exon variant	G/A	snv		6.9E-03	1
rs12024554	MICOS10 ; NBL1 ; MICOS10-NBL1	1	19599265	intron variant	C/T	snv		0.20	1
rs12078075	DSTYK	1	205194670	intron variant	G/A;C	snv			1
rs12131072	NR5A2	1	200088375	intron variant	C/A;T	snv			1
rs12138127	C1orf61	1	156433889	intron variant	C/G	snv		0.52	1
rs12138803	PIGC ; DNM3	1	172379683	intron variant	C/T	snv		0.23	1
rs12404660	WNT4	1	22132301	intron variant	A/G	snv		0.20	1
rs12740480	GTF2B	1	88886929	intron variant	T/A	snv		0.28	1
rs12757461		1	160446134	intergenic variant	G/A	snv		0.24	1
rs1289011		1	163656682	intergenic variant	C/A;G	snv			1
rs1415364	COL11A1	1	103087259	intron variant	C/T	snv		0.48	1
rs1535179	HNRNPR	1	23312516	intron variant	A/G	snv		7.1E-02	1
rs1563355	LYPLAL1-AS1 ; LOC107985272	1	219479759	intergenic variant	T/C	snv		0.61	1
rs17277127	DNM3	1	172167994	intron variant	A/T	snv		0.27	1